CA1074041A - Fire-retardant filled polypropylene composition - Google Patents
Fire-retardant filled polypropylene compositionInfo
- Publication number
- CA1074041A CA1074041A CA266,011A CA266011A CA1074041A CA 1074041 A CA1074041 A CA 1074041A CA 266011 A CA266011 A CA 266011A CA 1074041 A CA1074041 A CA 1074041A
- Authority
- CA
- Canada
- Prior art keywords
- parts
- polypropylene
- chlorinated polyethylene
- weight
- chlorinated
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
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Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/02—Halogenated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/22—Compounds containing nitrogen bound to another nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/10—Homopolymers or copolymers of propene
- C08L23/12—Polypropene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/10—Homopolymers or copolymers of propene
- C08L23/14—Copolymers of propene
- C08L23/142—Copolymers of propene at least partially crystalline copolymers of propene with other olefins
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/26—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers modified by chemical after-treatment
- C08L23/28—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers modified by chemical after-treatment by reaction with halogens or compounds containing halogen
- C08L23/286—Chlorinated polyethylene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L57/00—Compositions of unspecified polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C08L57/06—Homopolymers or copolymers containing elements other than carbon and hydrogen
- C08L57/08—Homopolymers or copolymers containing elements other than carbon and hydrogen containing halogen atoms
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
ABSTRACT
A filled polypropylene composition having excellent flame retardance is prepared by blending polypropylene resin with chlorinated paraffin hydrocarbon, chlorinated polyethylene, antimony oxide and alumina trihydrate. The compositions are compatible for molding and may be employed where flame retardance is of particular importance as for example for use as structural components in T.V. sets, radios and home appliances.
-i-
A filled polypropylene composition having excellent flame retardance is prepared by blending polypropylene resin with chlorinated paraffin hydrocarbon, chlorinated polyethylene, antimony oxide and alumina trihydrate. The compositions are compatible for molding and may be employed where flame retardance is of particular importance as for example for use as structural components in T.V. sets, radios and home appliances.
-i-
Description
~l 1074041 !l BACKGROUND OF THE INVENTION
The present invention relates to novel filled polypropy-¦lene compositions which are able to pass a more stringent flame l¦retardance test than ASTM D-635.
ll¦ In the past "flame retardant" polypropylene compositions, I i.e. those passing ASTM test D-635 have been prepared by incorpor-¦lation of chlorinated compounds into polypropylene resins. Addi-¦jtional flame retardants such as antimony oxide are often present '¦in these compositions for the purpose of further enhancing flame !retardancy.
¦l One group of chlorinated compounds that have been sug-¦lg~ested for such use, are the chlorinated paraffin hydrocarbons ¦¦containing between about 40 to 80~ chlorine and averaging 18 to 36 ¦Icarbon atoms. Although the chlorinated paraffin hydrocarbons can 15 ¦~ be added in small amounts to polypropylene without any particular iloperating problems, it has been found that when added in quantitie~
that should be sufficient for imparting acceptable flame retardanc~
according to present standards the chlorinated hydrocarbons are in-l~compatible with the polypropylene and will leach out during pro-20 ¦¦ cessing. The resultant tacky product will not pass a flame retar-¦dance test such as UL 94(1/1~) with V-l rating and will drip.
Another group of chlorinated compounds that is used a3 ,~flame retardants in polypropylene compositions are the chlorinated ¦¦polyethylenes containing between about 20 to 55 percent bound ¦chlorine. However, even when added to polypropylene in a 50:50 weight ratio together with antimony oxide it was found that the composition will not pass the aforementioned UL 94 test and will burn.
I In adding various inorganic filler such as glass, asbes-tos etc. to~po ypropylene containing any one of the aforementioned~
11 .
~_ .". . ._ _ : . ' ,: . , !l I
!l !
1! 1074041 chlorinated compounds, flame retardance is somewhat improved due to the dilution effect, however not to an acceptable level.
¦ Recently, compounds have been developed that act as-I! combined fillers and flame retardants for various resins. A charac-1l teristic common to these compounds is that they contain bound ¦Imoisture, which upon exposure of the filled resin to flame is re-,lleased as water vapor. Thus, these fillers act as a flame-inhibi-¦¦ting heat sink. One such filler-flame retardant of particular !linterest is alumina trihydrate, which is effective in various l¦thermoset resins, e.g. polyester, epoxies, phenolics and the like.
¦IHowever, due to the relatively low temperature at which water is ¦ liberated (230C), the use of alumina trihydrate is limited to ¦Iresins which can be processed, i.e. molded or cast, at temperaturec ~jwell below the decomposition temperature of the alumina trihydrate.
¦!This limitation has precluded the use of alumina trihydrate in ~polypropylene compositions, which are usually processed at higher !l temperatures.
1¦ It is therefore an object of this invention to provide ¦¦a filled polypropylene composition having improved flame retardanc~
!I properties and which can be processed without decomposition of the ¦Ifiller.
!l .
~I T~E INVENTION
,1 In accordance with the present invention there is pro-¦¦vided a composition which comprises polypropylene resin, chlorina-¦¦ted polyethylene, chlorinated paraffin hydrocarbon, antimony oxide ¦¦and alumina trihydrate.
I For purposes of this invention, polypropylene resin is ; I intended to cover homopolymer of propylene as well as various ~ copolymers of propylene and another ~ -olefin such as ethylene, 1 butylene and the like or mixtures of homopolymer and copolymer.
IIThe copolymers can be random copolymers or block copolymers where 1(~74041 'j~he blocks themselves may be either homopolymers or random copoly-mers. Also, included in the definition of polypropylene resin are various mixtures of propylene homopolymer or copolymer with a poly-l¦mer of at least one other ~-olefin such as ethylene. In general ¦the polymerized propylene content of these polypropylene resins ¦should be at least 75 percent by weight.
, The chlorinated polyethylene is one containing bound chlorine in a range from about 20 to about 55 percent by weight anc I can be derived from a polyethylene of any density. Chlorinated 1 polyethylenes are well known compounds, which are commercially available in a wide range of chlorine concentrations. Sufficient chlorinated polyethylene should be added to provide a weight ratio ¦thereof to polypropylene resin in the range of about 20:80 to 50:5 .
Il The chlorinated paraffin hydrocarbon should be one that ¦¦ contains on the average from about 18 to about 36 carbon atoms and between about 40 to about 80 percent by weight of bound chlo-rine. These compounds are commonly derived by chlorination of ! soft or slack waxes and are commercially available materials. The Iconcentration of chlorinated paraffin should be at least 15 parts, ,¦and preferably at least 20 parts per 100 parts of combined poly-propylene resin and chlorinated polyethylene.
Preferably, chlorinated polyethylene and chlorinated paraffin hydrocarbon should be added in sufficient quantities to !¦provide a chlorine concentration of at least 25 percent based on Ithe total weight of polypropylene resin, chlorinated polyethylene and chlorinated paraffinic hydrocarbon.
Antimony oxide is added for its known function in quan-tities of at least 5 partq per 100 parts of the combined weights l of polypropylene resin and chlorinated polyethylene.
¦ The alumina trihydrate component is used in the composi-¦¦tion of this invention in amounts of at least 20 parts by weight ¦per 100 parts of the combined weights of polypropylene resin and chlorinated polyethylene resin The preferred range is between -' " ' ;' ' ~ ' , " ,',, ~74041 about 35 and about 100 parts per 100 parts of the aformentioned resins.
The alumina trihydrate is a readily available material in that it is an intermediate product in the production of alumi-num metal. ~he average particle size of the trihydrate typically ranges from about 0.5 to about 25 microns. As a component of the composition of this invention it is preferred to use one having a relatively small average particle size e.g. from about 0.5 to about 5.
Other ingredients may also be added for purposes well known in the art. Such ingredients include plasticizers, dyes, pigments, lubricants, heat and light stabilizers, antioxidants, antistatic agent, synthetic or natural reinforcing fiber or fillers and the like.
The ccmponents of the composition may be blended using ; any of the well known techniques, e.g. by milling on a two-roll mill, by mixing in a Banbury mixer, by extrusion of dry blended components or any other technique employing temperatures below the decomposition temperature of alumina trihydrate.
It was unexpectedly found that in addition to being low smoke generating and able to meet the the stringent UL 94 test (1/16") with at least a V-l rating~ the composition in accordance with the present invention is readily processed at temperatures well below the decomposition temperature of alumina trihydrate, i.e. temperatures e.g. in the range of 35F to 400F. can be em-ployed in shaping various articles from the composition. Also, it was discovered that in this system the chlorinated paraffin hydrocarbon component was completely compatible upon molding, re-sulting in shaped articles of excellent quality and appearance.
The composition can be employed in a variety of applica-tions where flame retardance is a quality of particular importance.
Examples of such applications include the use as structural compon-ents in television sets, radios and various home appliances.
~0~4041 In order to provide a better understanding of the inven-~tion, reference is had to the following examples. Unless other-¦¦wise noted, all parts, proportions and percentages are expressed l¦in terms of weight.
1I EX.~MPLE 1 A mixture of 60 parts polypropylene homopolymer, 40 partC
chlorinated polyethylene ~containing 42% bound chlorine and avail-able under the trademark DOW 4213), 20 parts chlorinated paraffin ~ hydrocarbon (containing 70% bound chlorine and available under the 1 trade~ark CHLOREZ 70 HMP from Dover Chemical Corporation), 10 part antimony oxide, 40 parts alumina trihydrate having an average ¦ particle size of less than 1 micron (available under the trademark ¦HYDRAL 710 from Alcoa) and 5 parts stabilizers and lubricants was l¦compounded in a Banbury mixer at about 350F. The resulting com-l¦position passed the UL 94 1/16" flammability test with a V-0 rating and could easily be processed in subsequent molding operations without either decomposition of the alumina trihydrate or release ! of chlorinated paraffin hydrocarbon.
EX~MPLE 2 11 Another composition was prepared similarly except that the polypropylene resin was a copolymer of ethylene and propylene llhaving an ethylene content of about 3%, and 60 parts of the aluminc ¦~trihydrate was used. The composition had a flammability rating of ¦IV-1 (UL 94 1/16"j and excellent other physical properties: melt ¦!flow (2.16 kg at 190C) of 1.8 grams/10 min.,notched Izod impact of 8.5 ft.lbs./in., flexural strength of 2800 psi, flexural modulus o~
122,000 psi,tensile strength ~t yield of 2500 psi, tensile strengt~
¦at break of 1900 p9i and elongation of 117 Il _5_ ' .~
Il . .' . ~
. . .
In contrast, experiments with compositions containing polypropylene (homopolymer) and chlorinated polyethylene (trademark) DOW 2243.15, 48% bound chlorine) in a 50:50 weight ratio and con-taining 5-10 parts antimony oxide per 100 parts of the combined weight of polypropylene and chlorinated polyethylene, resulted in failure of the UL 94 1/16" flammability test and similar composi-tions also containing 25-40% glass fibers did not pass the afore-mentioned test.
Other experiments employing 60 parts of the polypropylene resin of Example 2 compounded with 40 parts alumina trihydrate re-sulted in compositions failing the flammability test. In addition, the polypropylene/alumina trihydrate compositions could not be processed, i.e~ molded, at conventional processing temperatures without decomposition of the alumina trihydrate. Other experiments with compositions containing 60 parts polypropylene, 40 parts chlorinated polyethylene, (42% bound chlorine), 20 parts chlorina-ted paraffin (70% bound chlorine) and 10 parts antimony oxide also resulted in inferior flammability ratings. When 30 parts glass fibers were also included in the latter compositions some improve-ment was noted, however, 40% of the tests still failed the flam-mability test.
While this invention has been described in detail for the purpose of illustration, it is not to be construed as limited thereby but is intended to cover all changes and modifications within the spirit and scope thereof.
:
The present invention relates to novel filled polypropy-¦lene compositions which are able to pass a more stringent flame l¦retardance test than ASTM D-635.
ll¦ In the past "flame retardant" polypropylene compositions, I i.e. those passing ASTM test D-635 have been prepared by incorpor-¦lation of chlorinated compounds into polypropylene resins. Addi-¦jtional flame retardants such as antimony oxide are often present '¦in these compositions for the purpose of further enhancing flame !retardancy.
¦l One group of chlorinated compounds that have been sug-¦lg~ested for such use, are the chlorinated paraffin hydrocarbons ¦¦containing between about 40 to 80~ chlorine and averaging 18 to 36 ¦Icarbon atoms. Although the chlorinated paraffin hydrocarbons can 15 ¦~ be added in small amounts to polypropylene without any particular iloperating problems, it has been found that when added in quantitie~
that should be sufficient for imparting acceptable flame retardanc~
according to present standards the chlorinated hydrocarbons are in-l~compatible with the polypropylene and will leach out during pro-20 ¦¦ cessing. The resultant tacky product will not pass a flame retar-¦dance test such as UL 94(1/1~) with V-l rating and will drip.
Another group of chlorinated compounds that is used a3 ,~flame retardants in polypropylene compositions are the chlorinated ¦¦polyethylenes containing between about 20 to 55 percent bound ¦chlorine. However, even when added to polypropylene in a 50:50 weight ratio together with antimony oxide it was found that the composition will not pass the aforementioned UL 94 test and will burn.
I In adding various inorganic filler such as glass, asbes-tos etc. to~po ypropylene containing any one of the aforementioned~
11 .
~_ .". . ._ _ : . ' ,: . , !l I
!l !
1! 1074041 chlorinated compounds, flame retardance is somewhat improved due to the dilution effect, however not to an acceptable level.
¦ Recently, compounds have been developed that act as-I! combined fillers and flame retardants for various resins. A charac-1l teristic common to these compounds is that they contain bound ¦Imoisture, which upon exposure of the filled resin to flame is re-,lleased as water vapor. Thus, these fillers act as a flame-inhibi-¦¦ting heat sink. One such filler-flame retardant of particular !linterest is alumina trihydrate, which is effective in various l¦thermoset resins, e.g. polyester, epoxies, phenolics and the like.
¦IHowever, due to the relatively low temperature at which water is ¦ liberated (230C), the use of alumina trihydrate is limited to ¦Iresins which can be processed, i.e. molded or cast, at temperaturec ~jwell below the decomposition temperature of the alumina trihydrate.
¦!This limitation has precluded the use of alumina trihydrate in ~polypropylene compositions, which are usually processed at higher !l temperatures.
1¦ It is therefore an object of this invention to provide ¦¦a filled polypropylene composition having improved flame retardanc~
!I properties and which can be processed without decomposition of the ¦Ifiller.
!l .
~I T~E INVENTION
,1 In accordance with the present invention there is pro-¦¦vided a composition which comprises polypropylene resin, chlorina-¦¦ted polyethylene, chlorinated paraffin hydrocarbon, antimony oxide ¦¦and alumina trihydrate.
I For purposes of this invention, polypropylene resin is ; I intended to cover homopolymer of propylene as well as various ~ copolymers of propylene and another ~ -olefin such as ethylene, 1 butylene and the like or mixtures of homopolymer and copolymer.
IIThe copolymers can be random copolymers or block copolymers where 1(~74041 'j~he blocks themselves may be either homopolymers or random copoly-mers. Also, included in the definition of polypropylene resin are various mixtures of propylene homopolymer or copolymer with a poly-l¦mer of at least one other ~-olefin such as ethylene. In general ¦the polymerized propylene content of these polypropylene resins ¦should be at least 75 percent by weight.
, The chlorinated polyethylene is one containing bound chlorine in a range from about 20 to about 55 percent by weight anc I can be derived from a polyethylene of any density. Chlorinated 1 polyethylenes are well known compounds, which are commercially available in a wide range of chlorine concentrations. Sufficient chlorinated polyethylene should be added to provide a weight ratio ¦thereof to polypropylene resin in the range of about 20:80 to 50:5 .
Il The chlorinated paraffin hydrocarbon should be one that ¦¦ contains on the average from about 18 to about 36 carbon atoms and between about 40 to about 80 percent by weight of bound chlo-rine. These compounds are commonly derived by chlorination of ! soft or slack waxes and are commercially available materials. The Iconcentration of chlorinated paraffin should be at least 15 parts, ,¦and preferably at least 20 parts per 100 parts of combined poly-propylene resin and chlorinated polyethylene.
Preferably, chlorinated polyethylene and chlorinated paraffin hydrocarbon should be added in sufficient quantities to !¦provide a chlorine concentration of at least 25 percent based on Ithe total weight of polypropylene resin, chlorinated polyethylene and chlorinated paraffinic hydrocarbon.
Antimony oxide is added for its known function in quan-tities of at least 5 partq per 100 parts of the combined weights l of polypropylene resin and chlorinated polyethylene.
¦ The alumina trihydrate component is used in the composi-¦¦tion of this invention in amounts of at least 20 parts by weight ¦per 100 parts of the combined weights of polypropylene resin and chlorinated polyethylene resin The preferred range is between -' " ' ;' ' ~ ' , " ,',, ~74041 about 35 and about 100 parts per 100 parts of the aformentioned resins.
The alumina trihydrate is a readily available material in that it is an intermediate product in the production of alumi-num metal. ~he average particle size of the trihydrate typically ranges from about 0.5 to about 25 microns. As a component of the composition of this invention it is preferred to use one having a relatively small average particle size e.g. from about 0.5 to about 5.
Other ingredients may also be added for purposes well known in the art. Such ingredients include plasticizers, dyes, pigments, lubricants, heat and light stabilizers, antioxidants, antistatic agent, synthetic or natural reinforcing fiber or fillers and the like.
The ccmponents of the composition may be blended using ; any of the well known techniques, e.g. by milling on a two-roll mill, by mixing in a Banbury mixer, by extrusion of dry blended components or any other technique employing temperatures below the decomposition temperature of alumina trihydrate.
It was unexpectedly found that in addition to being low smoke generating and able to meet the the stringent UL 94 test (1/16") with at least a V-l rating~ the composition in accordance with the present invention is readily processed at temperatures well below the decomposition temperature of alumina trihydrate, i.e. temperatures e.g. in the range of 35F to 400F. can be em-ployed in shaping various articles from the composition. Also, it was discovered that in this system the chlorinated paraffin hydrocarbon component was completely compatible upon molding, re-sulting in shaped articles of excellent quality and appearance.
The composition can be employed in a variety of applica-tions where flame retardance is a quality of particular importance.
Examples of such applications include the use as structural compon-ents in television sets, radios and various home appliances.
~0~4041 In order to provide a better understanding of the inven-~tion, reference is had to the following examples. Unless other-¦¦wise noted, all parts, proportions and percentages are expressed l¦in terms of weight.
1I EX.~MPLE 1 A mixture of 60 parts polypropylene homopolymer, 40 partC
chlorinated polyethylene ~containing 42% bound chlorine and avail-able under the trademark DOW 4213), 20 parts chlorinated paraffin ~ hydrocarbon (containing 70% bound chlorine and available under the 1 trade~ark CHLOREZ 70 HMP from Dover Chemical Corporation), 10 part antimony oxide, 40 parts alumina trihydrate having an average ¦ particle size of less than 1 micron (available under the trademark ¦HYDRAL 710 from Alcoa) and 5 parts stabilizers and lubricants was l¦compounded in a Banbury mixer at about 350F. The resulting com-l¦position passed the UL 94 1/16" flammability test with a V-0 rating and could easily be processed in subsequent molding operations without either decomposition of the alumina trihydrate or release ! of chlorinated paraffin hydrocarbon.
EX~MPLE 2 11 Another composition was prepared similarly except that the polypropylene resin was a copolymer of ethylene and propylene llhaving an ethylene content of about 3%, and 60 parts of the aluminc ¦~trihydrate was used. The composition had a flammability rating of ¦IV-1 (UL 94 1/16"j and excellent other physical properties: melt ¦!flow (2.16 kg at 190C) of 1.8 grams/10 min.,notched Izod impact of 8.5 ft.lbs./in., flexural strength of 2800 psi, flexural modulus o~
122,000 psi,tensile strength ~t yield of 2500 psi, tensile strengt~
¦at break of 1900 p9i and elongation of 117 Il _5_ ' .~
Il . .' . ~
. . .
In contrast, experiments with compositions containing polypropylene (homopolymer) and chlorinated polyethylene (trademark) DOW 2243.15, 48% bound chlorine) in a 50:50 weight ratio and con-taining 5-10 parts antimony oxide per 100 parts of the combined weight of polypropylene and chlorinated polyethylene, resulted in failure of the UL 94 1/16" flammability test and similar composi-tions also containing 25-40% glass fibers did not pass the afore-mentioned test.
Other experiments employing 60 parts of the polypropylene resin of Example 2 compounded with 40 parts alumina trihydrate re-sulted in compositions failing the flammability test. In addition, the polypropylene/alumina trihydrate compositions could not be processed, i.e~ molded, at conventional processing temperatures without decomposition of the alumina trihydrate. Other experiments with compositions containing 60 parts polypropylene, 40 parts chlorinated polyethylene, (42% bound chlorine), 20 parts chlorina-ted paraffin (70% bound chlorine) and 10 parts antimony oxide also resulted in inferior flammability ratings. When 30 parts glass fibers were also included in the latter compositions some improve-ment was noted, however, 40% of the tests still failed the flam-mability test.
While this invention has been described in detail for the purpose of illustration, it is not to be construed as limited thereby but is intended to cover all changes and modifications within the spirit and scope thereof.
:
Claims (9)
1. A flame retardant polypropylene composition which compri-ses:
a) polypropylene resin b) sufficient chlorinated polyethylene to provide a weight ratio of chlorinated polyethylene to polypropylene in the range from about 20:80 to about 50:50,said chlorinated polyethylene containing from about 20 to about 55 percent by weight bound chlorine;
c) at least 5 parts by weight of antimony oxide per 100 parts of the combined weights of polypropylene and chlorinated polyethylene;
d) at least 15 parts by weight of chlorinated paraffin hydrocarbon per 100 parts of the combined weights of polypropylene and chlorinated polyethylene, said chlorinated paraffin hydrocarbon containing on the average from about 18 to 36 carbon atoms per molecule and between about 40 to about 80 percent by weight bound chlorine.
e) at least 20 parts by weight of alumina trihydrate per 100 parts of the combined weights of polypropy-lene and chlorinated polyethylene.
a) polypropylene resin b) sufficient chlorinated polyethylene to provide a weight ratio of chlorinated polyethylene to polypropylene in the range from about 20:80 to about 50:50,said chlorinated polyethylene containing from about 20 to about 55 percent by weight bound chlorine;
c) at least 5 parts by weight of antimony oxide per 100 parts of the combined weights of polypropylene and chlorinated polyethylene;
d) at least 15 parts by weight of chlorinated paraffin hydrocarbon per 100 parts of the combined weights of polypropylene and chlorinated polyethylene, said chlorinated paraffin hydrocarbon containing on the average from about 18 to 36 carbon atoms per molecule and between about 40 to about 80 percent by weight bound chlorine.
e) at least 20 parts by weight of alumina trihydrate per 100 parts of the combined weights of polypropy-lene and chlorinated polyethylene.
2. The composition of claim 1 wherein the chlorine concentra-tion based on the total weight of polypropylene resin, chlorinated polyethylene and chlorinated paraffin hydrocarbon is at least 25 percent by weight.
3. A composition according to claim 1 wherein at least a portion of the polypropylene resin is a propylene homopolymer.
4. A composition according to claim 1 wherein at least a portion of the polypropylene is a copolymer of propylene and ano-ther ?-olefin.
5. A composition according to claim 1 wherein the concen-tration of chlorinated paraffin hydrocarbon is at least 20 parts per 100 parts of the combined weights of polypropylene resin and chlorinated polyethylene.
6. A composition according to claim 1 wherein the alumina trihydrate is present in concentrations ranging between about 35 and about 100 parts per 100 parts of the combined weights of poly-propylene resin and chlorinated polyethylene resin.
7. A composition according to claim 1 also containing rein-forcing fibers.
8. A composition according to claim 4 wherein the other ?-olefin is ethylene.
9. A composition according to claim 1 wherein the average particle size of the alumina trihydrate is between about 0.5 and about 5 microns.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/635,505 US4006114A (en) | 1975-11-26 | 1975-11-26 | Flame retardant polypropylene compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1074041A true CA1074041A (en) | 1980-03-18 |
Family
ID=24548061
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA266,011A Expired CA1074041A (en) | 1975-11-26 | 1976-11-18 | Fire-retardant filled polypropylene composition |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US4006114A (en) |
| JP (1) | JPS5265543A (en) |
| CA (1) | CA1074041A (en) |
| FR (1) | FR2333018A1 (en) |
| GB (1) | GB1508529A (en) |
| NO (1) | NO764032L (en) |
| SE (1) | SE414183B (en) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4096206A (en) * | 1976-02-09 | 1978-06-20 | Borg-Warner Corporation | Flame-retardant triazines |
| IT1102857B (en) * | 1977-10-05 | 1985-10-07 | Fochesato Antonio | PROCESS FOR THE PRODUCTION OF TEXTILE FIBERS AND NON-FLAMMABLE SYNTHETIC PARATEX PRODUCTS |
| JPS57158248A (en) * | 1981-03-27 | 1982-09-30 | Showa Denko Kk | Polyolefin composition |
| US4508640A (en) * | 1981-11-24 | 1985-04-02 | Showa Denko Kabushiki Kaisha | Electromagnetic wave-shielding materials |
| US5104604A (en) * | 1989-10-05 | 1992-04-14 | Dexter Electronic Materials Div. Of Dexter Corp. | Flame retardant epoxy molding compound, method and encapsulated device method of encapsulating a semiconductor device with a flame retardant epoxy molding compound |
| US5476716A (en) * | 1988-10-17 | 1995-12-19 | The Dexter Corporation | Flame retardant epoxy molding compound, method and encapsulated device |
| ES2202861T3 (en) * | 1997-05-28 | 2004-04-01 | Rockwool International A/S | AN INSULATING ELEMENT AND A PROCEDURE FOR PREPARATION. |
| DE60137760D1 (en) * | 2000-04-14 | 2009-04-09 | Sekisui Chemical Co Ltd | RESIN COMPOSITION FOR A VIBRATION DAMPING MATERIAL, VIBRATION DAMPING MATERIAL AND SOUND INSULATION ELEMENT |
| CN112608602A (en) * | 2020-12-03 | 2021-04-06 | 衡阳市盛亚化工科技有限公司 | Heat-resistant environment-friendly chlorinated paraffin |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2105187A1 (en) * | 1971-02-04 | 1972-08-10 | Veba Chemie Ag | Flame-resistant enamels |
| JPS52780B2 (en) * | 1973-05-07 | 1977-01-10 |
-
1975
- 1975-11-26 US US05/635,505 patent/US4006114A/en not_active Expired - Lifetime
-
1976
- 1976-11-18 CA CA266,011A patent/CA1074041A/en not_active Expired
- 1976-11-22 FR FR7635119A patent/FR2333018A1/en active Granted
- 1976-11-24 GB GB49010/76A patent/GB1508529A/en not_active Expired
- 1976-11-25 NO NO764032A patent/NO764032L/no unknown
- 1976-11-25 JP JP51140807A patent/JPS5265543A/en active Pending
- 1976-11-25 SE SE7613240A patent/SE414183B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| SE7613240L (en) | 1977-05-27 |
| GB1508529A (en) | 1978-04-26 |
| FR2333018A1 (en) | 1977-06-24 |
| NO764032L (en) | 1977-05-27 |
| SE414183B (en) | 1980-07-14 |
| JPS5265543A (en) | 1977-05-31 |
| US4006114A (en) | 1977-02-01 |
| FR2333018B1 (en) | 1981-02-06 |
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